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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2978 | carbohydrate metabolic disorder | RGD:1584008 | Rattus norvegicus (Norway rat) | 690163 | Oxct1 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:1584008 | Rattus norvegicus (Norway rat) | 690163 | Oxct1 |
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| DOID:9970 | obesity | RGD:1584008 | Rattus norvegicus (Norway rat) | 690163 | Oxct1 |
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| DOID:0081115 | benign familial infantile seizures 2 | MGI:1916267 | Mus musculus (house mouse) | 69017 | Prrt2 |
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| DOID:0090053 | episodic kinesigenic dyskinesia 1 | MGI:1916267 | Mus musculus (house mouse) | 69017 | Prrt2 |
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| DOID:0070423 | early onset progressive encephalopathy with brain atrophy and thin corpus callosum | HGNC:11581 | Homo sapiens (human) | 6904 | TBCD |
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| DOID:0080722 | Kenny-Caffey syndrome type 1 | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:0060348 | hypoparathyroidism-retardation-dysmorphism syndrome | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:11199 | hypoparathyroidism | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:9351 | diabetes mellitus | HGNC:11583 | Homo sapiens (human) | 6906 | SERPINA7 |
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| DOID:1459 | hypothyroidism | HGNC:11583 | Homo sapiens (human) | 6906 | SERPINA7 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11583 | Homo sapiens (human) | 6906 | SERPINA7 |
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| DOID:7998 | hyperthyroidism | HGNC:11583 | Homo sapiens (human) | 6906 | SERPINA7 |
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| DOID:1837 | diabetic ketoacidosis | HGNC:11583 | Homo sapiens (human) | 6906 | SERPINA7 |
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| DOID:0111837 | congenital nongoitrous hypothyroidism 8 | HGNC:11585 | Homo sapiens (human) | 6907 | TBL1X |
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| DOID:0050155 | sensory system disease | HGNC:11585 | Homo sapiens (human) | 6907 | TBL1X |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:0050967 | spinocerebellar ataxia type 17 | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:10652 | Alzheimer's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:0050847 | sleep apnea | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:12858 | Huntington's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:1289 | neurodegenerative disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:5419 | schizophrenia | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:162 | cancer | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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